Patent Application
20060228800
This invention relates to a means for regulation of gene function. More particularly, the present invention relates to a method and composition for generating an artificial intron and its components capable of producing microRNA (miRNA) molecules via intracellular RNA splicing and/or processing mechanisms, and thus inducing transgenic gene silencing effects of RNA interference (RNAi) on the cell or cells of a targeted organism, and the relative utilities thereof. The miRNA-producing intron so generated is useful for not only delivering desired miRNA function but also suppressing unwanted gene activity in the intron-mediated transgenic organism.
Therapeutic intervention of a genetic disease can be achieved by regulating specific disease-associated genes, such as replacing impaired gene functions or suppressing unwanted gene functions. Plasmids and viral vectors are commonly used for introducing active genes into a cell to repair impaired gene functions. To suppress unwanted gene functions, antisense oligonucleotides (U.S. Pat. No. 6,066,500 to Bennett) and small molecule drugs are often used as therapeutic agents. With the advance of recent RNA interference (RNAi) technologies, novel small RNA agents have been developed to provide more efficient and less toxic means in gene regulation, including utilization of long double-stranded RNA (dsRNA) (U.S. Pat. No. 6,506,599 to Fire), double-stranded short interfering RNA (siRNA) (Elbashir et. al. (2001) Nature 411: 494-498) and DNA-RNA interfering molecules (D-RNAi) (Lin et. al. (2001) Biochem. Biophys. Res. Commun. 281: 639-644), which may have great industrial and therapeutic applications.
The mechanism of RNAi elicits post-transcriptional gene silencing (PTGS) phenomena capable of inhibiting specific gene functions with high potency at a few nanomolar dosage, which has been proven to be effective longer and much less toxic than traditional gene therapies using antisense oligonucleotides or small molecule drugs (Lin et. al. (2001) Current Cancer Drug Targets 1: 241-247). Based on prior studies, the siRNA-induced gene silencing effect usually lasts up to one week, while that of D-RNAi can sustain over one month. These phenomena appear to evoke an intracellular gene sequence-specific RNA degradation process, affecting all highly homologous gene transcripts, called co-suppression. It has been proposed that such a co-suppression effect results from the generation of small RNA products (21˜25 nucleotide bases) by enzymatic activities of RNA-directed RNA polymerases (RdRp) and/or endoribonucleases III (RNaseIII) on aberrant RNA templates, which are derived from foreign transgenes or viral infections (Grant, S. R. (1999) Cell 96: 303-306; Lin et. al. (2001) supra; Bartel, D. P. (2004) Cell 116: 281-297; Lin et. al. (2004a) Drug Design Reviews 1: 247-255).
Although RNAi phenomena appear to offer a new avenue for suppressing gene function, the applications thereof have not been demonstrated to work constantly and safely in higher vertebrates, including avian, mammal and human. For example, findings of the siRNA-mediated RNAi effect are based on the use of double-stranded RNA (dsRNA), which has shown to cause interferon-induced non-specific RNA degradation in vertebrates (Stark et. al. (1998) Annu. Rev. Biochem. 67: 227-264; Elbashir et. al. supra; U.S. Pat. No. 4,289,850 to Robinson; and U.S. Pat. No. 6,159,712 to Lau). Such an interferon-induced cytotoxic response usually reduces the specificity of RNAi-associated gene silencing effects and results in global, non-specific RNA degradation in cells (Stark et. al. supra; Elbashir et. al. supra). Especially in mammalian cells, it has been noted that the gene silencing effects of RNAi are disturbed when the siRNA size is longer than 25 base-pairs (bp). Although transfection of siRNA or small hairpin RNA (shRNA) sized less than 21 bp may overcome such a problem, unfortunately for transgenic and therapeutic use, this limitation in size impairs the usefulness of siRNA and shRNA because it is difficult to deliver such small and unstable RNA constructs in vivo due to the abundant RNase activities in higher vertebrates (Brantl S. (2002) Biochimica et Biophysica Acta 1575: 15-25).
With the advance of transgenic methods in gene delivery, a functional gene is preferably transfected into a cell or an organism, such as plant, animal and human being, using gene-expressing vector vehicles, including retroviral vector, lentiviral vector, adenoviral vector, adeno-associated viral (AAV) vector and so on. The desirable gene function so obtained in the cell and organism is activated through gene transcription and subsequently translation to form a functional polypeptide or protein for compensating a gene dysfunction or for competing with the homologous gene function. The main purpose of such a vector-based transgenic approach is to maintain long-term gene modulation under the control of cellular transcription and translation machineries. However, prior vector-based transgenic technologies, including antisense oligonucleotide and dominant-negative gene inhibitor vectors, have been shown to involve tedious works in target selection and have frequently resulted in inconsistent and unstable effectiveness (Jen et. al. (2000) Stem Cells 18: 307-319).
Recent utilization of siRNA-expressing vectors has improved transgenic stability and offered relatively long-term RNAi effects on vector-based gene modulation (Tuschl et. al. (2002) Nat Biotechnol. 20: 446-448). Although prior arts (Miyagishi et. al. (2002) Nat Biotechnol 20: 497-500; Lee et. al. (2002) Nat Biotechnol 20: 500-505; Paul et. al. (2002) Nat Biotechnol 20: 505-508) attempting to use this siRNA approach have succeeded in maintaining constant gene silencing efficacy, their strategies failed to provide a specific RNAi effect on a targeted cell population because of the use of ubiquitous type III RNA polymerase (Pol-III) promoters. Pol-III promoters, such as U6 and H1, are activated in almost all cell types, making tissue-specific gene targeting impossible. Further, because the read-through effect of Pol-III activity occurs on a short transcription template in the absence of proper termination, large RNA products longer than desired 18-25 bp can be synthesized and cause unexpected interferon cytotoxicity (Gunnery et. al. (1995) Mol Cell Biol. 15: 3597-3607; Schramm et. al. (2002) Genes Dev 16: 2593-2620). Such a problem can also result from the competitive conflict between the Pol-III promoter and another vector promoter (i.e. LTR and CMV promoters). Sledz et al. and us have found that high dosage of siRNA (e.g., >250 nM in human T cells) caused strong cytotoxicity similar to that of dsRNA (Sledz et. al. (2003) Nat Cell Biol. 5: 834-839; Lin et al. (2004b) Intrn'l J. Oncol. 24: 81-88). This toxicity is due to the double-stranded structures of siRNA and dsRNA, which activates the interferon-mediated non-specific RNA degradation and programmed cell death through signaling via the PKR and 2-5A systems (Stark et. al. supra). Interferon-induced protein kinase PKR triggers cell apoptosis, while activation of interferon-induced (2′,5′)-oligoadenylate synthetase (2-5A) system leads to extensive cleavage of single-stranded RNAs (i.e. mRNAs). Both PKR and 2-5A systems contain dsRNA-binding motifs which are sensitive to dsRNA and siRNA, but not to single-strand microRNA (miRNA) or RNA-DNA duplex. Thus, these disadvantages limit the use of Pol-III-based RNAi vector systems in vivo.
In sum, in order to improve the delivery stability, targeting specificity and transgenic safety of modern vector-based RNAi technologies in vivo, a better induction and maintenance strategy is highly desired. Therefore, there remains a need for an effective, stable and safe gene modulation method as well as agent composition for regulating targeted gene function via the novel RNAi and/or PTGS mechanisms.
Research based on gene transcript (e.g. mRNA), an assembly of protein-coding exons, is fully described throughout the literature, taking the fate of spliced introns to be digested for granted (Clement et. al. (1999) RNA 5: 206-220; Nott et. al. (2003) RNA 9: 607-617). Is it true that the non-protein-coding intron is destined to be a metabolic waste without function or there is a function for it which has not yet been discovered? Recently, this misconception was corrected by the observation of intronic microRNA (miRNA). Intronic miRNA is a new class of small single-stranded regulatory RNAs derived from the processing of pre-mRNA introns. Approximately 10-30% of a spliced intron is exported into cytoplasm with a moderate half-life (Clement et. al. supra). miRNA is a single-stranded RNA molecule usually sized about 18-25 nucleotides (nt) in length and is capable of either directly degrading its intracellular messenger RNA (mRNA) target or suppressing the protein translation of its targeted mRNA, depending on the complementarity between the miRNA and its target. In this way, the intronic miRNA is functionally similar to previously described siRNA, but differs from them in the structural conformation and the requirement for Pol-II RNA transcription and splicing for its biogenesis (Lin et. al. (2003) Biochem Biophys Res Commun 310:754-760).
As shown in
Our present invention discloses a novel function of intron in the aspect of gene regulation and its relative utilities thereof. As shown in
In accordance with the present invention, the mature RNA molecule formed by the linkage of exons may be useful in conventional gene therapy to replace impaired or missing gene function, or to increase specific gene expression. Additionally, the present invention provide novel compositions and means in producing intracellular gene silencing molecules by way of RNA splicing and processing mechanisms to elicit either an antisense oligonucleotide effect or an RNA interference (RNAi) effect useful for inhibiting gene function. The RNA splicing- and processing-generated gene silencing molecules, such as antisense RNA, short temporary RNA (stRNA), double-stranded RNA (dsRNA), small interfering RNA (siRNA), short hairpin RNA (shRNA), microRNA (miRNA), tiny non-coding RNA (tncRNA), snRNA, snoRNA, and other RNAi-like small RNA constructs, resulting from the present invention is preferably used to target a gene selected from the group consisting of pathogenic nucleic acid, bacterial gene, viral gene, mutated gene, oncogene, jumping gene, transposon, microRNA gene and any other type of protein-coding as well as non-protein-coding genes.
In one preferred embodiment (
In another aspect, the recombinant gene of the present invention is constructed based on the natural pre-mRNA structure. The recombinant gene is consisted of two major different parts: exon and intron. The exon part is ligated after RNA splicing to form a functional mRNA and protein for tracking the release of the intronic RNA insert(s), while the intron part is spliced out of the recombinant gene transcript and further processed into a desired intronic RNA molecule, serving as the aforementioned antisense or RNAi molecule, including antisense RNA, miRNA, siRNA, shRNA and dsRNA, etc. These desired intronic RNA molecules may comprise at least a stem-loop structure containing a sequence domain homologous to (A/U)UCCAAGGGGG motifs, pre-miRNA loops or tRNA loops for accurate excision of the desired RNA molecule out of the intron and also for transporting the desired RNA molecule from nucleus to cytoplasm. The 5′-end of the intron contains a splicing donor site homologous to either GTAAGAGK or GU(A/G)AGU motifs, while its 3′-end is a splicing acceptor site that is homologous to either TACTWAY(N)mGWKSCYRCAG or CT(A/G)A(C/T)NG motifs, and preferably m≧1. The adenosine “A” nucleotide of the CT(A/G)A(C/T)NG sequence transcripts is part of (2′-5′)-linked branch-point acceptor formed by cellular (2′-5′)-oligoadenylate synthetases in eukaryotes, and the symbolic “N” nucleotide is either a nucleotide (e.g. deoxyadenosine, deoxyguanosine, deoxycytidine, deoxythymine, deoxyuridine, riboxyadenosine, riboxyguanosine, riboxycytidine, riboxythymine and riboxyuridine) or an oligonucleotide, most preferably a T- and/or C-rich oligonucleotide sequence. There could be a linker nucleotide sequence for the connection of the stem-loop to either a splicing donor or acceptor site, or both.
In another preferred embodiment of the present invention (
In one aspect, the recombinant gene, for example, encoding an antisense RNA molecule as shown in
To produce small RNA molecules, such as siRNA, miRNA and shRNA, via RNA splicing and processing mechanisms, an expression-competent vector may be needed for stable transfection and expression of the intron-containing pre-mRNA molecule. The desired RNA molecule is produced intracellularly by promoter-driven mRNA transcription and then released by the RNA splicing and processing machineries. The expression-competent vector can be any nucleotide composition selected from a group consisting of plasmid, cosmid, phagemid, yeast artificial chromosome, transposon, jumping gene, retroviral vector, lentiviral vector, lambda vector, AMV, CMV, AAV, modified Hepatitis-virus vector, plant-associated mosaic viruses, and a combination thereof. The expression of the pre-mRNA is driven by either a viral or a cellular RNA polymerase promoter, or both. For example, a lentiviral or retrovirual LTR promoter is sufficient to provide up to 5×105 copies of pre-mature mRNA per cell, while a CMV promoter can transcribe over 106 to 108 copies of pre-mature mRNA per cell. It is feasible to insert a drug-sensitive repressor element in front of the lentiviral/retroviral or CMV promoter in order to control their transcription rate and timing. The repressor element can be inhibited by a chemical drug or antibiotics selected from the group of G418, tetracycline, neomycin, ampicillin, kanamycin, etc, and a combination thereof.
The desired RNA molecule can be either homologous or complementary, or both, to a targeted RNA transcript or a part of the RNA transcript of a gene selected from the group consisted of fluorescent protein gene, luciferase gene, lac-Z gene, microRNA gene, miRNA precursor, transposon, jumping gene, viral gene, bacterial gene, insect gene, plant gene, animal gene, human genes, protein-coding as well as non-protein-coding genes, and their homologues, and a combination thereof. The complementary and/or homologous region of the desired RNA molecule is sized from about 12 to about 2,000 nucleotide bases, most preferably in between about 18 to about 27 nucleotide bases. The desired RNA molecule may also contain the combination of homologous and complementary sequences to an RNA transcript or a part of the RNA transcript, such as a palindromic sequence capable of forming secondary hairpin-like structures. The homology and/or complementarity rate is ranged from about 30˜100%, more preferably 35˜49% for a desired hairpin-RNA conformation and 90˜100% for both desired sense- and antisense-RNA molecules.
The present invention provides a novel means of producing aberrant RNA molecules in cell as well as in vivo, including dsRNA, siRNA, miRNA, tncRNA and shRNA compositions in vivo to induce RNAi/PTGS-associated gene silencing phenomena. Hence, the present invention provides a novel intronic RNA transcription, splicing and processing method for producing long or short sense, antisense, or both in haipin-like conformation, RNA molecules with pre-determined length and specificity. The desired intronic RNA molecule after intracellular splicing and processing can be produced in single unit or in multiple units on the recombinant gene transcript of the present invention. Same or different spliced RNA products can be generated in either sense or antisense orientation, or both, complementary to the mRNA transcript(s) of a target gene. In certain case, spliced RNA molecules complementary to a gene transcript (i.e. mRNA) can be hybridized through intracellular formation of double-stranded RNA (dsRNA) for triggering either RNAi-related phenomena with short siRNA (≦25 bp) or interferon-induced cytotoxicity with long (>25 bp) dsRNA. In other case, any small-interfering RNA (siRNA), microRNA (miRNA) and short-hairpin RNA (shRNA) molecules, or a combination thereof, can be produced as small spliced RNA molecules for inducing the RNAi/PTGS-associated gene silencing effect. The siRNA, miRNA and shRNA so obtained can be constantly produced by an expression-competent vector in vivo, thus, alleviate concerns of fast small RNA degradation. The RNA splicing-processed molecule obtained from cell culture can also be isolated and purified in vitro for generating either dsRNA or deoxyribonucleotidylated RNA (D-RNA) that is capable of triggering RNAi and/or PTGS phenomena when the molecule is transfected into a cell or an organism.
Alternatively, the present invention further provides a novel means for producing antisense microRNA (miRNA*) directed against a targeted microRNA (miRNA) in eukaryotes, resulting in inhibition of the miRNA function. Because the miRNA functions RNAi-associated gene silencing, the miRNA* can neutralize this gene silencing effect and thus rescue the function of the miRNA-suppressed gene(s). Unlike perfectly matched siRNA, the binding of miRNA* to miRNA creates a mismatched base-paired region for miRNA cleavage and degradation. Such a mismatched base-paired region is preferably located either in the middle of the stem-arm region or in the stem-loop structure of the miRNA precursor (pre-miRNA). It has been shown that mismatched base-pairing in the middle of siRNA inhibits the gene silencing effect of the siRNA (Holen et. al. (2002) Nucleic Acid Res. 30: 1757-1766; Krol et. al. (2004) J. Biol. Chem. 279: 42230-42239). Probably similar to intron-mediated enhancement (IME) phenomena in plants, previous studies in Arabidopsis and Nicotiana spp. have indicated that intronic inserts play an important role in posttranscriptional gene modulation (Rose, A. B. (2002) RNA 8: 1444-1451). The IME mechanism can recover targeted gene expression from 2 fold to over 10 fold by targeting the miRNA for silencing, which is complementary to the targeted gene.
The
The
Referring particularly to the drawings for the purpose of illustration only and not limitation, there is illustrated:
FIGS. 10A-B show the Northern blot analysis of SpRNAi-induced cellular gene silencing against HIV-1 infection as described in Example 7.
FIGS. 12A-C show different designs of intronic RNA inserts in an SpRNAi construct for microRNA biogenesis and the resulting gene silencing of targeted green fluorescent protein (EGFP) expression in zebrafish, demonstrating an asymmetric design preference in transfection of (1) 5′-miRNA*-stemloop-miRNA-3′ and (2) 5′-miRNA-stemloop-miRNA*-3′ hairpin RNA structures, respectively, as described in Example 9.
FIGS. 13A-B show the generation of transgenic loss-of-FMRP-gene-function zebrafish in vivo, using the present invention for disease model research as described in Example 10. Because the Tg(UAS:gfp) zebrafish expresses green GFP and the anti-FMRP SpRNAi transgene is marked with red GFP, we can easily observe the normal dendritic neurons (green) versus the loss-of-FMRP-function neurons (yellow) in fish brain.
FIGS. 14A-D show the gene silencing effects of the Example 11 on organ development in transgene-like chicken embryos, including liver and skin with β-catenin gene knockout (A)-(C) and beak with noggin gene knockdown (D) in vivo.
FIGS. 16A-B show the Northern blot analysis of HIV gene silencing using the present invention as described in Example 13. Complete suppression of HIV-1 replication using SpRNAi transfection against gag/pro/pol viral genes in patients' CD4+ T lymphocytes was observed, indicating a feasible vaccination strategy for AIDS therapy and treatment of viral infection.
Although specific embodiments of the present invention will now be described with reference to the drawings, it should be understood that such embodiments are by way of example only and merely illustrative of but a small number of the many possible specific embodiments which can represent applications of the principles of the present invention. Various changes and modifications obvious to one skilled in the art to which the present invention pertains are deemed to be within the spirit, scope and contemplation of the present invention as further defined in the appended claims.
The present invention provides a novel composition and method for altering genetic characteristics of a cell or an organism. Without being bound by any particular theory, such an alteration of genetic characteristics is directed to a newly discovered intron-mediated gene silencing mechanism, triggered by transfection of an artificially recombinant gene containing at least an RNA splicing- and processing-competent intron (SpRNAi) construct in the cell or organism of interest. The SpRNAi intron carries an intronic RNA insert, which can be released by intracellular RNA splicing and processing machineries and then triggers RNAi and/or PTGS-related gene silencing effects on complementary gene targets. Generally, as shown in
Similar to natural mRNA splicing and processing processes, the spliceosome machinery catalyzing intron removal in our design of the present invention is formed by sequential assembly of intracellular spliceosomal components on several snRNP-recognition elements of the SpRNAi intron (e.g. binding sites for snRNPs U1, U2 and U4/U6.U5 tri-snRNP). The methods for incorporating synthetic snRNP-recognition elements in an SpRNAi intron are described in Examples 2 and 3. In brief, a sequential assembly of the snRNPs to their recognition elements has been proposed: first, binding of U1 snRNP to the 5′-splicing junction (splicing donor site), then binding of U2 snRNP to a branch-point site, and last, association of the U4/U6.U5 tri-snRNP to the U1 and U2 snRNPs, so as to form an early splicing complex for precisely cleavage of the 5′-splicing junction. On the other hand, the 3′-splicing junction (splicing acceptor site) is cleaved by a late splicing complex formed by U5 snRNP and some other splicing proteins after the release of the 5′-splicing junction. However, little is known about the protein/protein and RNA/protein interactions that bridge the U4/U6 and U5 snRNP components within a eukaryotic tri-snRNP, and knowledge on the binding sites of proteins on U4/U6 and U5 snRNPs remains largely unclear.
Design of Artificially Recombinant Genes for Testing Intron-Mediated Gene Silencing Effects
Strategy for molecular analysis of intracellular RNA splicing- and processing-directed gene silencing mechanisms was tested using an artificial recombinant gene, namely SpRNAi-rGFP (
The SpRNAi intron is flanked with a splicing donor (DS) and acceptor (AS) site, and contains at least one anti-gene insert, a branch point (BrP) and a poly-pyrimidine tract (PPT) in between the DS-AS sites for interacting with intracellular spliceosomes. Using low stringent Northern blotting analysis (middle bottom of
As shown in
The splicing donor site is an oligonucleotide motif containing homology to (5′-exon-AG)-(splicing point)-GTA(A/-)GAG(G/T)-3′ sequences (SEQ.ID.NO.1), including but not limited, 5′-AG GTAAGAGGAT-3′, 5′-AG GTAAGAGT-3′, 5′-AG GTAGAGT-3′, 5′-AG GTAAGT-3′, etc. The splicing acceptor site is another oligonucleotide motif comprising homology to 5′-G(W/-)(T/G)(C/G)C(T/C)(G/A)CAG-(splicing point)-(G/C-3′-exon) sequences (while W is a pyrimidine A, T or U) (SEQ.ID.NO.2), including but not limited, 5′-GATATCCTGCAG G-3′, 5′-GGCTGCAG G-3′, 5′-CCACAG C-3′, etc. The branch point is an “A” nucleotide located within an oligonucleotide element/domain homologous to 5′-TACT(A/T)A*(C/T)(-/C)-3′ sequences (while the symbol “*” marks the branch site) (SEQ.ID.NO.3), including but not limited, 5′-TACTAAC-3′, 5′-TACTTATC-3′ and so on. The poly-pyrimidine tract is a high T or C content oligonucleotide sequence homologous to 5′-(TY)m(C/-)(T)nC(C/-)-3′ or 5′-(TC)nNCTAG(G/-)-3′ (while Y is a C or T/U and the “-” means an empty site). The symbols of “m” and “n” indicates multiple repeats ≧1; most preferably, m=1˜3 and n=7˜12. For all of the above spliceosomal recognition components, the deoxythymidine (T) nucleotide is replaceable with a uridine (U).
To test the function of a spliced intron, various oligonucleotide inserts were cloned into the SpRNAi through restriction/cloning sites, respectively. The restriction/cloning site is preferably generated by a restriction enzyme selected from the group of AatII, AccI, AflII/III, AgeI, ApaI/LI, AseI, Asp718I, BamHI, BbeI, BclI/II, BglII, BsmI, Bsp120I, BspHI/LU11I/120I, BsrI/BI/GI, BssHII/SI, BstBI/UI/XI, ClaI, Csp6I, DpnI, DraI/II, EagI, Ecl136II, EcoRI/RII/47III, EheI, FspI, HaeIII, HhaI, HinPI, HindIII, HinfI, HpaI/II, KasI, KpnI, MaeII/III, MfeI, MluI, MscI, MseI, NaeI, NarI, NcoI, NdeI, NgoMI, NotI, NruI, NsiI, PmlI, Ppu 101, PstI, PvuI/II, RsaI, SacI/II, SalI, Sau3AI, SmaI, SnaBI, SphI, SspI, StuI, TaiI, TaqI, XbaI, XhoI, XmaI endonuclease, and a combination thereof. These intron inserts are DNA templates encoding aberrant RNAs selected from the group consisting of lariat-form RNA, short-temporary RNA (stRNA), antisense RNA, small-interfering RNA (siRNA), double-stranded RNA (dsRNA), short-hairpin RNA (shRNA), microRNA (miRNA), aberrant RNA containing mismatched base pairing, long deoxynucleotidylated RNA (D-RNA), ribozyme RNA and their precursors as well as derivatives in either sense or antisense orientation, or both, and a combination thereof.
As shown in Example 5, the expression of a hairpin-like RNA insert from SpRNAi-rGFP often induces a much stronger gene silencing effect than those of sense and antisense RNA inserts, showing an average of >80% knockdown specificity to all targeted gene transcripts. This knockdown specificity is determined by both of the complementarity and homology between the intronic insert and its targeted gene transcript. For example, the most effective hairpin-SpRNAi insert often possessed about 40˜42% homology and 40˜42% complementarity to the targeted gene domain, while an A/T-rich linker sequence filled in the rest 6˜20% space as a loop conformation. To those sense- and antisense-SpRNAi inserts, although the homology or complementarity can be increased up to 100% in one orientation, an average of 40˜50% knockdown efficacy was observed. Therefore, depending on the homology and complementarity between the intronic insert and the targeted gene transcript, we can design and use different kinds of intronic inserts, either respectively or together, to manipulate specific gene expression at a desired level in the cell or organism of interest.
Simultaneous Expression of rGFP and Silencing of eGFP by SpRNAi Transfection
For the convenience of gene delivery and activation in tested cells or organisms, an SpRNAi-containing recombinant gene is preferably cloned into an expression-competent vector, selected from the group consisting of plasmid, cosmid, phagmid, yeast artificial chromosome, transposon, jumping gene, viral vector, and the combination thereof. The vector is introduced into the cell, tissue, plant or animal organism by a high efficient gene delivery method selected from the group consisting of liposomal transfection, chemical transfection, chemical transformation, electroporation, transposon recombination, jumping gene insertion, viral vector infection, micro-injection, gene-gun penetration, and a combination thereof.
As shown in
As shown in
Western Blot Analysis of RNA Splicing- and Processing-Directed eGFP Silencing Effects
As shown in
Western Blot Analysis of RNA Splicing- and Processing-Directed Integrin β1 Silencing in Human Prostatic Cancer Cells
As shown in
Strategy for HIV Vaccination Using SpRNAi-rGFP Vector Transfection
Northern blot analysis of SpRNAi-mediated gene silencing directed against HIV-promoted cellular genes is shown to inhibit HIV infection (FIGS. 10A-B). Feasibility of AIDS vaccination was tested using SpRNAi-derived intronic miRNA directed against cellular genes as anti-HIV drugs.
Because CD4 has normal function in IL-2 stimulation and T-cell growth activation, the CD4 receptor may not be an ideal target for HIV prevention. However, the search for HIV-dependent cellular genes in vivo was hindered by the fact that infectivity of viruses and infection rate among different patients are usually different leading to inconsistent results. Short-term ex-vivo culture conditions can normalize infectivity and infection rate of HIV transmission in a more uniform CD4+ T cell population. Microarray analysis based on such ex vivo conditions would be reliable for critical biomedical and genetic research of HIV-1 infection. Our studies of microarray-identified differential gene profiles between HIV− and HIV+ T cells in the acute and chronic infection phases has provided many potential anti-HIV cellular gene targets for AIDS therapy and prevention. To functionally evaluate the usefulness of targeting cellular genes for HIV vaccination, three highly differentially expressed genes, Naf1β, Nb2 homologous protein to Wnt-6 (Nb2HP) and Tax1 binding protein (Tax1BP), has been tested to inhibit HIV-1 infectivity.
Because each of them contributes only parts of AIDS complications, knockdown of single target gene failed to suppress HIV-1 infection, while combination of all three SpRNAi drugs at the same total concentration showed a significant 80±10% reduction of HIV-1 infection (p<0.01). As shown in
Different Mechanisms Between siRNA-Mediated and SpRNAi-Mediated RNAi
Although an in vitro model of siRNA-mediated RNAi has been proposed, the characteristics of Dicer and RNA-induced silencing complex (RISC) are distinctly different in the siRNA and miRNA mechanisms (Tang, G. (2005) Trends Biochem Sci. 30: 106-114).
Intron-Mediated Gene Silencing in Zebrafish In Vivo
The foregoing discussion establishes the fact that intronic miRNAs are effective strategy for silencing targeted gene expression in vivo. We first tried to determine the structural design of pre-miRNA inserts for the best gene silencing effect. We found that a strong structural preference presents in the selection of mature miRNA for assembly of the RNAi effector, RNA-induced gene silencing complex (RISC). RISC is a protein-RNA complex that directs either targeted gene transcript degradation or translational repression through the RNAi mechanism.
In zebrafish, we have observed that the stem-loop structure of pre-miRNA determines the sequence of mature miRNA for RISC assembly, which is different from siRNA-associated RISC assembly (Lin et. al. (2005) Gene 356: 32-38). Formation of siRNA duplexes plays a key role in assembly of the siRNA-associated RISC. The two strands of the siRNA duplex are functionally asymmetric, but assembly into the RISC complex is usually preferential for only one strand. Such a preference is determined by the thermodynamic stability of each 5′-end base-pairing in the siRNA strand. Based on this siRNA model, the formation of miRNA and its complementary miRNA (miRNA*) duplex was thought to be an essential step for the assembly of miRNA-associated RISC. If this were true, no functional bias would be observed in the stem-loop structure of pre-miRNA. However, we observed that the stem-loop of the intronic pre-miRNA was involved in the strand selection of a mature miRNA for RISC assembly.
In experiments, we constructed miRNA-expressing SpRNAi-RGFP vectors as described in Example 3 and two symmetric pre-miRNAs, miRNA-stemloop-miRNA* (1) and miRNA*-stemloop-miRNA (2), were synthesized and inserted into the vectors, respectively. Both pre-miRNAs contained the same double-stranded stem-arm region, which was directed against the EGFP nt 280-302 sequence. Because the intronic insert region of the SpRNAi-RGFP recombined gene is flanked with a PvuI and an MluI restriction site at the 5′- and 3′-ends, respectively, the primary insert can be easily removed and replaced by various anti-gene inserts (e.g. anti-EGFP) possessing cohesive ends. By allowing changes in the SpRNAi insert directed against different gene transcripts, this intronic miRNA biogenesis system provides a valuable tool for genetic and miRNA-associated research in vivo.
To determine the structural preference of the designed pre-miRNAs, we isolated the zebrafish small RNAs by mirVana miRNA isolation columns (Ambion, Austin, Tex.) and then precipitated all potential miRNAs complementary to the target EGFP region by latex beads containing the target RNA sequence. One full-length miRNA, miR-EGFP(280-302), was verified to be active in transfection of the 5′-miRNA-stemloop-miRNA*-3′ construct, as shown in
The indicator RGFP (red) was evenly detected in the fish transfected by either (1) or (2) pre-miRNA, whereas the silencing effect on targeted EGFP (green) was observed only in the fish transfected by the 5′-miRNA-stemloop-miRNA*-3′ (2) pre-miRNA, showing a mixed orange rather than wildtype yellow color. As shown in
Generation of Novel Transgenic Animal Models In Vivo Using the Present Invention
Fragile X syndrome (FraX) is the most common form of inherited mental retardation, with the estimated prevalence of 30% of total human mental retardation disorders, and is also among the most frequent single gene disorders. The gene affected by the syndrome in 99% patients, FMR1, is transcriptionally inactivated by the expansion and the methylation of trinucleotide (CGG) repeats, located in the 5′-untranslated region (5′-UTR) of the gene. This 5UTR r(CGG) expansion region was proposed to be the native anti-FMR1 microRNA target site of human FraX disorder (Jin et al. (2004) Nat Cell Biol. 6: 1048-1053). Native anti-FMR1 miRNA triggers the formation of RNA-induced initiator of transcriptional gene silencing (RITS) on the homologous (CGG) repeats and leads to heterochromatin repression of the FMR1 locus. FMR1 encodes an RNA-binding protein, FMRP, which is associated with polyribosome assembly in an RNA-dependent manner and capable of suppressing protein translation through an RNA interference (RNAi)-like pathway that is important for neuronal development and plasticity. However, no appropriate animal model is available for the study of FraX etiology because current Drosophila and mouse models are all based on the gene deletion of FMRP, completely irrelevant to the mechanism of RNAi.
To investigate the role of microRNA (miRNA) in this proposed disease model, we have designed and tested man-made miRNA transgenes directed against the fish fmr1 gene to generate loss-of-function transgenic zebrafish. After transgenic transfection as shown in
As shown in
Intron-Mediated Gene Silencing in Chicken Embryos
The in vivo model of chicken embryos has been widely utilized in many developmental biology, signal transduction and flu vaccine development research. We thus successfully tested the feasibility of transgene-like gene silencing in chicken in vivo using intronic RNA and discovered that a coupled interaction of nascent pre-mRNA transcription and intron excision occurring proximal to genomic perichromatin fibrils may be essential for microRNA (miRNA) biogenesis. The SpRNAi intron can be integrated into a host gene for transgenic expression. In an effort to examine such a transgenic model of intronic miRNA, we transfected chicken embryos with an isolated RCAS SpRNAi construct containing a hairpin anti-β-catenin pre-miRNA insert, which was directed against the protein-coding region of the chicken β-catenin gene sequence (NM205081). As an example, the β-catenin gene was selected because its products play a critical role in the biological development. β-catenin is known to be involved in the growth control of skin and liver tissues in chicken.
As shown in
After ten days of primordial injection, the embryonic chicken livers showed an enlarged and engorged first lobe, but the size of the second and third lobes of the livers were dramatically decreased (
In another attempt to silence noggin expression in the chicken mandible beak area using a similar approach (
Intron-Mediated Gene Silencing in Mouse Skins
To test the intronic miRNA effect on adult mammals (
Thus, utilization of intronic miRNA expression vectors provides a powerful new strategy for in-vivo gene therapy, particularly for melanoma treatment. Under the same dosage, Pol-II-mediated miRNA did not cause detectable cytotoxicity, whereas Pol-III-directed siRNA induced non-specific mRNA degradation as previous reports (Sledz et. al. supra; Lin (2004b) supra). This underscores the fact that miRNA is effective in vivo without the cytotoxic effect of double-stranded RNA. This result also indicates that the miRNA gene silencing effect is stable and efficient in knocking down the target gene expression over a relatively long time since hair regrowth requires at least a ten-day period of time to reach full recovery. Advantageously, intronic miRNA offers relatively long-term, effective and safe gene manipulation in local animal tissues and organs, preventing the lethal effect of systemic gene knockouts used in the conventional transgenic animal models. The same approach and strategy can be used to increase milk production in cow, to increase meat production in cattle and pig, to generate big size animals or small size pets, and to develop large size as well as weather-resistant plants.
Anti-Viral Therapy Using Intron-Mediated Gene Silencing Against Foreign Transgenes
During the early HIV infection, the viral reverse transcriptase transcribes the HIV RNA genome into a double-stranded cDNA sequence, which forms a pre-integration complex with the matrix, integrase and viral protein R (Vpr). This complex is then transferred to the cell nucleus and integrated into the host chromosome, consequently establishing the HIV provirus. We hypothesized that, although HIV carries few reverse transcriptase and matrix proteins during its first entry into host cells, the co-suppression of Pr55gag and p66/p51pol gene expression by miRNA would eliminate the production of infectious viral particles in the late infection phase. Silencing Pr55gag may prevent the assembly of intact viral particles due to the lack of matrix and capsid proteins, while suppression of protease in p66/p51pol can inhibit the maturation of several viral proteins. HIV expresses about nine viral gene transcripts which encode at least 15 various proteins; thus, the separation of a polyprotein into individual functional proteins requires the viral protease activity.
The anti-HIV SpRNAi-rGFP vector was tested in CD4+ T lymphocyte cells from HAART-treated, HIV-seropositive patients. Because only partial complementarity between miRNA and its target RNA is needed to trigger the gene silencing effect, this approach may be superior to current small molecule drugs since the high rate of HIV mutations often produces resistance to such agents. Northern blot analysis in
Sequencing analysis has revealed at least two HIV-1 mutants in the acute phase and seven HIV-1 mutants in the chronic phase within the targeted HIV genome domain. It is likely that the higher genome complexity produced by HIV mutations in chronic infections reduces miRNA-mediated silencing efficacy. Transfection of 50 nM miRNA*-expressing vector containing homology to the HIV-1 genome however reverses the RNAi effect on viral genome, indicating the specificity of the SpRNAi-derived miRNA and miRNA* effects (lanes 4 and 5). Expression of cellular house-keeping gene, β-actin, was normal and showed no interferon-induced non-specific RNA degradation. These results suggest that the anti-HIV SpRNAi-rGFP vector is highly specific and efficient in suppressing HIV-1 replication in early infections. In conjunction with an intermittent interleukin-2 (IL-2) therapy, the growth of non-infected CD4+ T lymphocytes can be stimulated to eliminate the HIV-infected cells, demonstrating a very promising pharmaceutical and therapeutic approach for AIDS therapy. The same approach and strategy can be used for the development of vaccine and therapy against other viral infection, such as hepatitis B virus (HBV), hepatitis C virus (HCV), herpes virus (HPV), smallpox virus, flu virus and so on.
Recovery of miRNA-Suppressed Gene Expression by Antisense microRNA (miRNA*)
Our studies of SpRNAi utilities also demonstrated that an intron-mediated enhancement (IME) phenomenon, similar to that reported in plants, takes place in mammalian cells. Previous studies in Arabidopsis and Nicotiana spp., indicate that introns play an important role in posttranscriptional gene modulation for both enhancing and silencing specific gene expression. When certain intronic sequences were inserted into an intronless gene, the expression of such gene transcripts was steadily increased ranging from 2 fold to over 10 fold. The intron-mediated increase of gene expression is usually at the level of mRNA accumulation although its mechanism remains to be elucidated.
We have tested the transfection of SpRNAi-rGFP genes containing inserts homologous to the first in-frame intron at the nts 43˜68 region of integrin β1 (ITGb1) in human cervical cancer HeLa cells, which express a moderate amount of ITGb1 adhesion protein consistent with elevated cell proliferation and metastatic activity. The increase of ITGb1 expression potentially restricts the spreading of cervical cancer cells in situ because alterations of cellular characteristics were observed through the attachment of cancer cells to a glycine-coated culture dish surface.
A. Definitions
To facilitate understanding of the invention, a number of terms are defined below:
Nucleotide: a monomeric unit of DNA or RNA consisting of a sugar moiety (pentose), a phosphate, and a nitrogenous heterocyclic base. The base is linked to the sugar moiety via the glycosidic carbon (1′ carbon of the pentose) and that combination of base and sugar is a nucleoside. A nucleoside containing at least one phosphate group bonded to the 3′ or 5′ position of the pentose is a nucleotide.
Oligonucleotide: a molecule comprised of two or more deoxyribonucleotides or ribonucleotides, preferably more than three, and usually more than ten. The exact size will depend on many factors, which in turn depends on the ultimate function or use of the oligonucleotide. The oligonucleotide may be generated in any manner, including chemical synthesis, DNA replication, reverse transcription, or a combination thereof.
Nucleic Acid: a polymer of nucleotides, either single or double stranded.
Nucleotide Analog: a purine or pyrimidine nucleotide that differs structurally from A, T, G, C, or U, but is sufficiently similar to substitute for the normal nucleotide in a nucleic acid molecule.
Gene: a nucleic acid whose nucleotide sequence codes for an RNA and/or a polypeptide (protein). A gene can be either RNA or DNA.
Base Pair (bp): a partnership of adenine (A) with thymine (T), or of cytosine (C) with guanine (G) in a double stranded DNA molecule. In RNA, uracil (U) is substituted for thymine. Generally the partnership is achieved through hydrogen bonding.
Precursor messenger RNA (pre-mRNA): primary ribonucleotide transcripts of a gene, which are produced by type-II RNA polymerase (Pol-II) machineries in eukaryotes through an intracellular mechanism termed transcription. A pre-mRNA sequence contains a 5′-end untranslated region, a 3′-end untranslated region, exons and introns.
Intron: a part or parts of a gene transcript sequence encoding non-protein-reading frames.
Exon: a part or parts of a gene transcript sequence encoding protein-reading frames.
Messenger RNA (mRNA): assembly of pre-mRNA exons, which is formed after intron removal by intranuclear spliceosomal machineries and served as a protein-coding RNA for protein synthesis.
cDNA: a single stranded DNA that is complementary to an mRNA sequence and does not contain any intronic sequences.
Sense: a nucleic acid molecule in the same sequence order and composition as the homologous mRNA. The sense conformation is indicated with a “+”, “s” or “sense” symbol.
Antisense: a nucleic acid molecule complementary to the respective mRNA molecule. The antisense conformation is indicated as a “−” symbol or with an “a” or “antisense” in front of the DNA or RNA, e.g., “aDNA” or “aRNA”.
5′-end: a terminus lacking a nucleotide at the 5′ position of successive nucleotides in which the 5′-hydroxyl group of one nucleotide is joined to the 3′-hydroyl group of the next nucleotide by a phosphodiester linkage. Other groups, such as one or more phosphates, may be present on the terminus.
3′-end: a terminus lacking a nucleotide at the 3′ position of successive nucleotides in which the 5′-hydroxyl group of one nucleotide is joined to the 3′-hydroyl group of the next nucleotide by a phosphodiester linkage. Other groups, most often a hydroxyl group, may be present on the terminus.
Template: a nucleic acid molecule being copied by a nucleic acid polymerase. A template can be single-stranded, double-stranded or partially double-stranded, depending on the polymerase. The synthesized copy is complementary to the template, or to at least one strand of a double-stranded or partially double-stranded template. Both RNA and DNA are synthesized in the 5′ to 3′ direction. The two strands of a nucleic acid duplex are always aligned so that the 5′ ends of the two strands are at opposite ends of the duplex (and, by necessity, so then are the 3′ ends).
Nucleic Acid Template: a double-stranded DNA molecule, double stranded RNA molecule, hybrid molecules such as DNA-RNA or RNA-DNA hybrid, or single-stranded DNA or RNA molecule.
Conserved: a nucleotide sequence is conserved with respect to a pre-selected (reference) sequence if it non-randomly hybridizes to an exact complement of the pre-selected sequence.
Complementry or Complementarity or Complementation: used in reference to polynucleotides (i.e., a sequence of nucleotides) related by the base-pairing rules. For example, the sequence “A-G-T” is complementary to the sequence “T-C-A,” and also to “T-C-U.” Complementation can be between two DNA strands, a DNA and an RNA strand, or between two RNA strands. Complementarity may be “partial” or “complete” or “total”. Partial complementarity or complementation occurs when only some of the nucleic acid bases are matched according to the base pairing rules. Complete or total complementarity or complementation occurs when the bases are completely matched between the nucleic acid strands. The degree of complementarity between nucleic acid strands has significant effects on the efficiency and strength of hybridization between nucleic acid strands. This is of particular importance in amplification reactions, as well as in detection methods that depend on binding between nucleic acids. Percent complementarity or complementation refers to the number of mismatch bases over the total bases in one strand of the nucleic acid. Thus, a 50% complementation means that half of the bases were mismatched and half were matched. Two strands of nucleic acid can be complementary even though the two strands differ in the number of bases. In this situation, the complementation occurs between the portion of the longer strand corresponding to the bases on that strand that pair with the bases on the shorter strand.
Homologous or Homology: refers to a polynucleotide sequence having similarities with a gene or mRNA sequence. A nucleic acid sequence may be partially or completely homologous to a particular gene or mRNA sequence, for example. Homology may also be expressed as a percentage determined by the number of similar nucleotides over the total number of nucleotides.
Complementry Bases: nucleotides that normally pair up when DNA or RNA adopts a double stranded configuration.
Complementry Nucleotide Sequence: a sequence of nucleotides in a single-stranded molecule of DNA or RNA that is sufficiently complementary to that on another single strand to specifically hybridize between the two strands with consequent hydrogen bonding.
Hybridize and Hybridization: the formation of duplexes between nucleotide sequences which are sufficiently complementary to form complexes via base pairing. Where a primer (or splice template) “hybridizes” with target (template), such complexes (or hybrids) are sufficiently stable to serve the priming function required by a DNA polymerase to initiate DNA synthesis. There is a specific, i.e. non-random, interaction between two complementary polynucleotides that can be competitively inhibited.
RNA interference (RNAi): a posttranscriptional gene silencing mechanism in eukaryotes, which can be triggered by small RNA molecules such as microRNA and small interfering RNA. These small RNA molecules usually function as gene silencers, interfering with expression of intracellular genes containing either completely or partially complementarity to the small RNAs.
MicroRNA (miRNA): single-stranded RNAs capable of binding to targeted gene transcripts that have partial complementarity to the miRNA. miRNA is usually about 16-28 oligonucleotides in length and is able to either directly degrade its intracellular mRNA target(s) or suppress the protein translation of its targeted mRNA, depending on the complementarity between the miRNA and its target mRNA. Natural miRNA molecules are found in almost all eukaryotes, functioning as a defense against viral infections and allowing regulation of gene expression during development of plants and animals.
MicroRNA* (miRNA*): single-stranded RNA containing partial or complete complementarity to the sequence of a mature microRNA.
Small interfering RNA (siRNA): short double-stranded RNAs sized about 18-25 perfectly base-paired ribonucleotide duplexes and capable of degrading target gene transcripts with almost perfect complementarity.
Short hairpin RNA (shRNA): single-stranded RNA that contains a pair of partially or completely matched stem-arm nucleotide sequences divided by an unmatched oligonucleotide loop to form a hairpin-like structure. Many natural miRNA products are derived from hairpin-like RNA precursors, namely precursor microRNA (pre-miRNA).
Vector: a recombinant nucleic acid molecule such as recombinant DNA (rDNA) capable of movement and residence in different genetic environments. Generally, another nucleic acid is operatively linked therein. The vector can be capable of autonomous replication in a cell in which case the vector and the attached segment is replicated. One type of preferred vector is an episome, i.e., a nucleic acid molecule capable of extrachromosomal replication. Preferred vectors are those capable of autonomous replication and/or expression of nucleic acids to which they are linked. Vectors capable of directing the expression of genes encoding for one or more polypeptides are referred to herein as “expression vectors”. Particularly important vectors allow cloning of cDNA from mRNA produced using a reverse transcriptase.
Cistron: a sequence of nucleotides in a DNA molecule coding for an amino acid residue sequence and including upstream and downstream DNA expression control elements.
Promoter: a nucleic acid to which a polymerase molecule recognizes, perhaps binds to, and initiates synthesis. For the purposes of the instant invention, a promoter can be a known polymerase binding site, an enhancer and the like, any sequence that can initiate synthesis by a desired polymerase.
Antibody: a peptide or protein molecule having a pre-selected conserved domain structure coding for a receptor capable of binding a pre-selected ligand.
B. Compositions
A recombinant nucleic acid composition for inducing intron-mediated gene silencing comprises:
(1) At least an intron, wherein said intron is flanked with a plurality of exons and can be cleaved out of the exons by intracellular RNA splicing and/or processing machineries; and
(2) A plurality of exons, wherein said exons can be linked to form a gene possessing a desired function.
The above recombinant nucleic acid composition, further comprises:
(1) At least a restriction/cloning site, wherein said restriction/cloning site is used for inserting the recombinant nucleic acid composition into an expression-competent vector for expressing the RNA transcript of said recombinant nucleic acid composition in a desired cell or organism; and
(2) A plurality of transcription and translation termination sites, wherein said transcription and translation termination sites are used for produce the correct RNA transcript sizes of said recombinant nucleic acid composition.
The intron of the above recombinant nucleic acid composition, further comprises:
(1) A gene-specific insert complementary or homologous to a targeted gene;
(2) A splicing donor site;
(3) A splicing acceptor site;
(4) A branch point domain for spliceosomal recognition;
(5) At least a poly-pyrimidine tract for spliceosomal interaction; and
(6) linkers for connection of the above major components.
The splicing donor site is a nucleotide motif homologous to (5′-exon-AG)-(splicing point)-GTA(A/-)GAG(G/T)-3′ sequences (SEQ.ID.NO.1), including but not limited, 5′-AG GTAAGAGGAT-3′, 5′-AG GTAAGAGT-3′, 5′-AG GTAGAGT-3′, and 5′-AG GTAAGT-3′ etc. The splicing acceptor site is another kind of a nucleotide motif homologous to 5′-G(W/-)(T/G)(C/G)C(T/C)(G/A)CAG-(splicing point)-(G/C-3′-exon) sequences (while W is a pyrimidine A, T or U) (SEQ.ID.NO.2), including but not limited, 5′-GATATCCTGCAG G-3′, 5′-GGCTGCAG G-3′, and 5′-CCACAG C-3′ etc. The branch point is an “A” nucleotide located within a sequence homologous to 5′-TACT(A/T)A*(C/T)(-/C)-3′ (while the symbol “*” marks the branch site) (SEQ.ID.NO.3), including but not limited, 5′-TACTAAC-3′, 5′-TACTTATC-3′ and so on. The poly-pyrimidine tract is a high T or C content oligonucleotide sequence homologous to 5′-(TY)m(C/-)(T)nC(C/-)-3′ or 5′-(TC)nNCTAG(G/-)-3′ (while Y is a C or T/U and the “-” means an empty site). The symbols of “m” and “n” indicates multiple repeats ≧1; most preferably, m=1˜3 and n=7˜12. For all the above spliceosomal recognition components, the deoxythymidine (T) is replaceable with a uridine (U).
C. Methods
A method for inducing intron-mediated gene silencing effects comprises:
(1) Constructing a recombinant nucleic acid composition containing at least an intron flanked with a plurality of exons, wherein said intron can be cleaved out of the exons by RNA splicing and/or processing for gene silencing and said exons can be linked together to form a mature gene transcript with or without a desired function;
(2) Cloning said recombinant nucleic acid composition into an expression-competent vector;
(3) Introducing said vector into a cell or an organism;
(4) Generating RNA transcript of said recombinant nucleic acid composition; and
(5) Releasing the functional part(s) of said intron via intracellular RNA splicing and/or processing mechanisms, so as to provide gene silencing effects against a targeted gene or genes containing sequences complementary to said intron.
Alternatively, a method for inducing RNA interference and/or posttranscriptional gene silencing effects comprises:
(1) Constructing a recombinant gene containing a functional RNA polymerase promoter and at least an intron flanked with a plurality of exons, wherein said intron can be cleaved out of the exons by RNA splicing and/or processing for gene silencing and said exons can be linked together to form a mature gene transcript with or without a desired function;
(2) Introducing said recombinant gene into a cell or an organism;
(3) Generating RNA transcript of said recombinant gene; and
(4) Releasing the functional parts of said intron via RNA splicing and/or processing mechanisms, so as to provide gene silencing effects against a targeted gene or genes containing sequences complementary to said intron.
More broadly, a method for suppressing gene function or silencing gene expression, comprising the steps of:
(1) providing: i) a substrate expressing a targeted gene, and ii) a nucleic acid composition comprising a recombinant gene capable of producing a specific RNA transcript, which is in turn able to generate pre-designed gene silencing molecules through intracellular RNA splicing and/or processing mechanisms to inhibit the targeted gene expression or suppress the targeted gene function in the substrate;
(2) treating the substrate with the nucleic acid composition under conditions such that the targeted gene expression or function in the substrate is inhibited.
Various changes and modifications obvious to one skilled in the art to which the present invention pertains are deemed to be within the spirit, scope and contemplation of the present invention as further defined in the appended claims.
The following examples serve to illustrate certain preferred embodiments and aspects of the present invention and are not to be construed as limiting the scope thereof.
In the experimental disclosure which follows, the following abbreviations apply: M (molar); mM (millimolar); μm (micromolar); mol (moles); pmol (picomolar); gm (grams); mg (milligrams); μg (micrograms); ng (nanograms); L (liters); ml (milliliters); μl (microliters); ° C. (degrees Centigrade); cDNA (copy or complementary DNA); DNA (deoxyribonucleic acid); ssDNA (single stranded DNA); dsDNA (double-stranded DNA); dNTP (deoxyribonucleotide triphosphate); RNA (ribonucleic acid); PBS (phosphate buffered saline); NaCl (sodium chloride); HEPES (N-2-hydroxyethylpiperazine-N-2-ethanesulfonic acid); HBS (HEPES buffered saline); SDS (sodium dodecylsulfate); Tris-HCl (tris-hydroxymethylaminomethane-hydrochloride); and ATCC (American Type Culture Collection, Rockville, Md.).
Rat neuronal stem cell clones AP31 and PZ5a were primary cultured and maintained as described by Palmer et. al., (J. Neuroscience, 1999). The cells were grown on polyornathine/laminin-coated dishes in DMEM/F-12 (1:1; high glucose) medium containing 1 mM L-glutamine supplemented with 1×N2 supplements (Gibco/BRL, Gaithersburg, Md.) and 20 ng/ml FGF-2 (Invitrogen, Carlsbad, Calif.), without serum at 37° C. under 5% CO2. For long-term primary cultures, 75% of the medium was replaced with new growth medium every 48 hr. Cultures were passaged at ˜80% confluency by exposing cells to trypsin-EDTA solution (Irvine Scientific) for 1 min and rinsing once with DMEM/F-12. Detached cells were replated at 1:10 dilution in fresh growth medium supplemented with 30% (v/v) conditioned medium which had exposed to cells for 24 hr before passaging. Human prostatic cancer LNCaP cells were obtained from the American Type Culture Collection (ATCC) and grown in RPMI 1640 medium supplemented with 10% fetal bovine serum with 100 μg/ml gentamycin at 37° C. under 10% CO2. The LNCaP culture was passaged at 80% confluency by exposing cells to trypsin-EDTA solution for 1 min and rinsing once with RPMI, and detached cells were replated at 1:10 dilution in fresh growth medium. After 48-hour incubation, RNA from tested cells was isolated by RNeasy spin columns (Qiagen, Valencia, Calif.), fractionated on a 1% formaldehyde-agarose gel, and transferred onto nylon membranes. The genomic DNA was also isolated by apoptotic DNA ladder kit (Roche Biochemicals, Indianapolis, Ind.) and assessed by 2% agarose gel electrophoresis, while cell growth and morphology were examined by microscopy and cell counting.
Synthetic nucleic acid sequences used for generation of three different SpRNAi introns containing either sense-, antisense- or hairpin-eGFP insert were listed as followings: N1-sense, 5′-pGTAAGAGGAT CCGATCGCAG GAGCGCACCA TCTTCTTCAA GA-3′ (SEQ.ID.NO.4); N1-antisense, 5′-pCGCGTCTTGA AGAAGATGGT GCGCTCCTGC GATCGGATCC TCTTAC-3′ (SEQ.ID.NO.5); N2-sense, 5′-pGTAAGAGGAT CCGATCGCTT GAAGAAGATG GTGCGCTCCT GA-3′ (SEQ.ID.NO.6); N2-antisense, 5′-pCGCGTCAGGA GCGCACCATC TTCTTCAAGC GATCGGATCC TCTTAC-3′ (SEQ.ID.NO.7); N3-sense, 5′-pGTAAGAGGAT CCGATCGCAG GAGCGCACCA TCTTCTTCAA GTTAACTTGA AGAAGATGGT GCGCTCCTGA-3′ (SEQ.ID.NO.8); N3-antisense, 5′-pCGCGTCAGGA GCGCACCATC TTCTTCAAGT TAACTTGAAG AAGATGGTGC GCTCCTGCGA TCGGATCCTC TTAC-3′ (SEQ.ID.NO.9); N4-sense, 5′-pCGCGTTACTA ACTGGTACCT CTTCTTTTTT TTTTTGATAT CCTGCAG-3′ (SEQ.ID.NO.10); N4-antisense, 5′-pGTCCTGCAGG ATATCAAAAA AAAAAGAAGA GGTACCAGTT AGTAA-3′ (SEQ.ID.NO.11). Additionally, two exon fragments were generated by DraII restriction enzyme cleavage of red fluorescent rGFP gene (SEQ.ID.NO.12) at its 208th nucleotide (nt) site and the 5′ fragment was further blunt-ended by T4 DNA polymerase. The rGFP referred to a new red-fluorescin chromoprotein generated by insertion of an additional aspartate at the 69th amino acid (aa) of HcRed1 chromoproteins from Heteractis crispa, developing less aggregate and almost twice intense far-red fluorescent emission at the ˜570-nm wavelength. This mutated rGFP gene sequence was cloned into pHcRed1-N1/1 plasmid vector (BD Biosciences, Palo Alto, Calif.) and propagated with E. coli DH5α LB-culture containing 50 μg/ml kanamycin (Sigma Chemical, St. Louis, Mo.). We cleaved the pHcRed1-N1/1 plasmid with XhoI and XbaI restriction enzymes and purified a 769-bp rGFP fragment and a 3,934-bp empty plasmid separately from 2% agarose gel electrophoresis.
Hybridization of N1-sense to N1-antisense, N2-sense to N2-antisense, N3-sense to N3-antisense and N4-sense to N4-antisense was separately performed by heating each complementary mixture of sense and antisense (1:1) sequences to 94° C. for 2 min and then 70° C. for 10 min in 1×PCR buffer (e.g. 50 mM Tris-HCl, pH 9.2 at 25° C., 16 mM (NH4)2SO4, 1.75 mM MgCl2). Continuously, sequential ligation of either N1, N2 or N3 hybrid to the N4 hybrid was performed by gradually cooling the mixture of N1-N4, N2-N4 or N3-N4 (1:1) hybrids respectively from 50° C. to 10° C. over a period of 1 hr, and then T4 ligase and relative buffer (Roche) were mixed with the mixture for 12 hr at 12° C., so as to obtain introns for insertion into exons with proper ends. After the rGFP exon fragments were added into the reaction (1:1:1), T4 ligase and buffer were adjusted accordingly to reiterate ligation for another 12 hr at 12° C. For cloning the right sized recombinant rGFP gene, 10 ng of the ligated nucleotide sequences were amplified by PCR with rGFP-specific primers 5′-dCTCGAGCATG GTGAGCGGCC TGCTGAA-3′ (SEQ.ID.NO.13) and 5′-dTCTAGAAGTT GGCCTTCTCG GGCAGGT-3′ (SEQ.ID.NO.14) at 94° C., 1 min, 52°, 1 min and then 68° C., 2 min for 30 cycles. The resulting PCR products were fractionated on a 2% agarose gel, and a ˜900-bp nucleotide sequences was extracted and purified by gel extraction kit (Qiagen). The composition of this ˜900 bp SpRNAi-containing rGFP gene was further confirmed by sequencing.
Because the recombinant gene possessed an XhoI and an XbaI restriction site at its 5′- and 3′-end, respectively, it can be easily cloned into a vector with corresponding ends complementary to the XhoI and XbaI cloning sites. The vector was an expressing-capable organism or suborganism selected from the group consisted of plasmids, cosmids, phagmids, yeast artificial chromosomes, jumping genes, transposons and viral vectors. Moreover, since the insert within the intron was flanked with a PvuI and an MluI restriction site at its 5′- and 3′-end, respectively, we can remove and replace the insert with another different insert sequence possessing corresponding ends complementary to the PvuI and MluI cloning sites. The insert sequence was homologous or complementary to a gene fragment selected from the group consisted of fluorescent protein (GFP) genes, luciferase genes, lac-Z genes, viral genes, bacterial genes, plant genes, animal genes and human genes. The homology and/or complementarity rate is ranged from about 30˜100%, more preferably 35˜49% for a hairpin-like shRNA insert and 90˜100% for both sense-stRNA and antisense-siRNA inserts.
For cloning into plasmids, since the SpRNAi-recombinant rGFP gene possessed an XhoI and an XbaI restriction site at its 5′- and 3′-end, respectively, it can be easily cloned into a vector with relatively complementary ends to the XhoI and XbaI cloning sites. We mixed the SpRNAi-recombinant rGFP gene and the linearized 3,934-bp empty pHcRed1-N1/1 plasmid at 1:16 (w/w) ratio, cooled the mixture from 65° C. to 15° C. over a period of 50 min, and then added T4 ligase and relative buffer accordingly into the mixture for ligation at 12° C. for 12 hr. This formed an SpRNAi-recombinant rGFP-expressing plasmid (SpRNAi-rGFP) vector, which can be propagated in E. coli DH5a LB-culture containing 50 μg/ml kanamycin. A positive clone was confirmed by PCR reaction with rGFP-specific primers SEQ.ID.NO.13 and SEQ.ID.NO.14 at 94° C., 1 min and then 68° C., 2 min for 30 cycles, and further sequencing. For cloning into viral vectors, the same ligation procedure was performed except using an XhoI/XbaI-linearized pLNCX2 retroviral vector (BD) instead. Since the insert within the SpRNAi intron was flanked with a PvuI and a MluI restriction site at its 5′- and 3′-end, respectively, we removed and replaced the eGFP insert with various integrin β1-specific insert sequences possessing corresponding ends complementary to the PvuI and MluI cloning sites.
Synthetic nucleic acid sequences used for generation of various SpRNAi introns containing either sense-, antisense- or hairpin-integrin β1 insert were listed as followings: P1-sense, 5′-pCGCAAGCAGG GCCAAATTGT GGGTA-3′ (SEQ.ID.NO.15); P1-antisense, 5′-pTAGCACCCAC AATTTGGCCC TGCTTGTGCG C-3′ (SEQ.ID.NO.16); P2-sense, 5′-pCGACCCACAA TTTGGCCCTG CTTGA-3′ (SEQ.ID.NO.17); P2-antisense, 5′-pTAGCCAAGCA GGGCCAAATT GTGGGTTGCG C-3′ (SEQ.ID.NO.18); P3-sense, 5′-pCGCAAGCAGG GCCAAATTGT GGGTTTAAAC CCACAATTTG GCCCTGCTTG A-3′ (SEQ.ID.NO.19); P3-antisense, 5′-pTAGCACCCAC AATTTGGCCC TGCTTGAATT CAAGCAGGGC CAAATTGTGG GTTGCGC (SEQ.ID.NO.20). These inserts were designed using Gene Runner software v3.0 (Hastings, Calif.) and formed by hybridization of P1-sense to P1-antisense, P2-sense to P2-antisense and P3-sense to P3-antisense, targeting the 244˜265th-nt sequence of integrin P1 gene (NM 002211.2). The SpRNAi-containing rGFP-expressing retroviral vector can be propagated in E. coli DH5a LB-culture containing 100 μg/ml ampcillin (Sigma). We also used a packaging cell line PT67 (BD) for producing infectious, replication-incompetent virus. The transfected PT67 cells were grown in DMEM medium supplemented with 10% fetal bovine serum with 4 mM L-glutamine, 1 mM sodium pyruvate, 100 μg/ml streptomycin sulfate and 50 μg/ml neomycin (Sigma) at 37° C. under 5% CO2. The titer of virus produced by PT67 cells was determined to be at least 106 cfu/ml before transfection.
RNA (20 μg of total RNA or 2 μg poly[A+] RNA) was fractionated on 1% formaldehyde-agarose gels and transferred onto nylon membranes (Schleicher & Schuell, Keene, N.H.). A synthetic 75-bp probe (5′-dCCTGGCCCCC TGCTGCGAGT ACGGCAGCAG GACGTAAGAG GATCCGATCG CAGGAGCGCA CCATCTTCTT CAAGT-3′ (SEQ.ID.NO.21)) targeting the junction region between rGFP and the anti-eGFP insert was labeled with the Prime-It II kit (Stratagene, La Jolla, Calif.) by random primer extension in the presence of [32P]-dATP (>3000 Ci/mM, Amersham International, Arlington Heights, Ill.), and purified with 30 bp-cutoff Micro Bio-Spin chromatography columns (Bio-Rad, Hercules, Calif.). Hybridization was carried out in the mixture of 50% freshly deionized formamide (pH 7.0), 5× Denhardt's solution, 0.5% SDS, 4×SSPE and 250 mg/mL denatured salmon sperm DNA fragments (18 hr, 42° C.). Membranes were sequentially washed twice in 2×SSC, 0.1% SDS (15 min, 25° C.), and once in 0.2×SSC, 0.1% SDS (15 min, 25° C.) before autoradiography.
For interference of eGFP gene expression, we transfected rat neuronal stem cells with SpRNAi-rGFP plasmid vectors encoding either sense, antisense or hairpin anti-eGFP insert, using a Fugene reagent (Roche). Plasmids containing insert-free rGFP gene and SpRNAi-recombinant rGFP gene with an insert against HIV gag-p24 were used as negative control. Cell morphology and fluorescence imaging was photographed at 0-, 24- and 48-hour time points after transfection. At the 48-hr incubation time point, the rGFP-positive cells were sorted by flow cytometry and collected for Western blot analysis. For interference of integrin β1 expression, we transfected LNCaP cells with pLNCX2 retroviral vectors containing various SpRNAi-rGFP genes directed against the 244˜265th-nt domain of integrin β1 using the Fugene reagent. The transfection rate of pLNCX2 retroviral vector into LNCaP cells was tested to be about 20%, while the pLNCX2 virus was less infectious to LNCaP cells. The same analyses were performed as aforementioned.
For immunoblotting, cells were rinsed with ice cold PBS after growth medium was removed, and then treated with the CelLytic-M lysis/extraction reagent (Sigma) supplemented with protease inhibitors, Leupeptin, TLCK, TAME and PMSF, following manufacture's recommendations. The cells were incubated at room temperature on a shaker for 15 min, scraped into microtubes, and centrifuged for 5 min at 12,000×g to pellet the cell debris. Protein-containing cell lysate were collected and stored at −70° C. until use. Protein determinations were measured with SOFTmax software package on an E-max microplate reader (Molecular Devices, Sunnyvale, Calif.). Each 30 μg cell lysate was added into SDS-PAGE sample buffer either with (reduced) or without (unreduced) 50 mM DTT, and boiled for 3 min before loaded onto 8% polyacylamide gels, while the reference lane was loaded with 2˜3 μl molecular weight markers (Bio-Rad). SDS-polyacrylamide gel electrophoresis was performed according to the standard protocols (Molecular Cloning, 3rd ED). Protein fractionations were electroblotted onto a nitrocellulose membrane, blocked with Odyssey blocking reagent (Li-Cor Biosciences, Lincoln, Nebr.) for 1˜2 hr at the room temperature. We assessed GFP expression using primary antibodies directed against eGFP (1:5,000; JL-8, BD) or rGFP (1:10,000; BD), overnight at 4° C. The blot was then rinsed 3 times with TBS-T and exposed to a secondary antibody, goat anti-mouse IgG conjugate with Alexa Fluor 680 reactive dye (1:2,000; Molecular Probes), for 1 hr at the room temperature. After three more TBS-T rinses, scanning and image analysis were completed with Li-Cor Odyssey Infrared Imager and Odyssey Software v.10 (Li-Cor). For integrin β1 analysis, the same procedure was performed except using primary antibodies directed against integrin β1 (1:2,000; LM534, Chemicon, Temecula, Calif.).
To clone the SpRNAi-rGFP recombinant genes into viral vectors, the same ligation procedure was performed using pLNCX2 retroviral vector (BD) as described in Example 3. Because the intronic insert in SpRNAi was flanked with a PvuI and an MluI restriction site at the 5′- and 3′-ends, respectively, we can remove and replace the anti-eGFP inserts with a different anti-gene insert possessing cohesive ends to the PvuI and MluI restriction site. The inserts were designed using Gene Runner software v3.0 (Hastings, Calif.) and formed by hybridization of each pair of sense and antisense synthetic oligonucleotides, targeting the first exon sequence of either Naf1β (AJ011896), Nb2HP(H12458) or Tax1BP (U25801) gene. The SpRNAi-rGFP-expressing retroviral vector, namely SpRNAi-pLNCX2, was propagated in E. coli DH5α LB-culture containing 100 μg/ml ampcillin (Sigma). We can also use a PT67 packaging cell line (BD) for producing infectious, replication-incompetent virus. The transfected PT67 cells were grown in DMEM medium supplemented with 10% fetal bovine serum (BSA) with 4 mM L-glutamine, 1 mM sodium pyruvate, 100 μg/ml streptomycin sulfate and 50 μg/ml neomycin (Sigma) at 37° C. under 5% CO2. The titer of virus produced by PT67 cells was determined to be over 5×106 cfu/ml before transfection.
CD4+ T lymphocytes were isolated from peripheral blood mononuclear cells of normal donors using immunomagnetic beads (Miltenyi Biotec, Auburn, Calif.) and cultured in RPMI 1640 medium supplemented with 20% BSA, 4 μg/ml phytohemagglutinin and 50 U/ml recombinant human IL-2 (Roche) at 37° C., 10% CO2. For anti-HIV vaccination, SpRNAi-pLNCX2 provirus (˜6×106 cfu/ml) in 100 μl of RPMI 1640 medium was applied to 2 ml medium (about 30 nM) in suspension flasks containing ˜800 T cells/μl. One day prior to infection, the culture medium was replaced with medium containing 2% fetal bovine serum and 200 U/ml IL-2 for 30 hr. After that, to establish HIV infection, the T cells with or without SpRNAi-pLNCX2 transfection (˜150 cell/μl) were mixed with supernatants collected from pooled HIV-seropositive T cell extracts from HAART-treated patients. Viral supernatants contained ˜3×105 total viral RNA copies/ml, approximate to FDA standards established for appearance of AIDS symptoms. Infection occurred at an MOI of 0.1. Viral stock solutions confirmed to Virology Quality Assurance Standards for infection and were diluted in plasma collected from HIV-seronegative donors. Viral aliquotes were stored at −80° C. until needed for infection. ELISA detection (Roche;
The RNA-polymerase cycling reaction (RNA-PCR) procedure can be modified to synthesize mRNA-cDNA, DNA-aRNA, DNA-cDNA and mRNA-aRNA duplex hybrids as transgenes, isolated from an SpRNAi recombinant gene, the template of an expression-competent vector or a transcriptome source (Lin et. al. (1999) Nucleic Acids Res. 27: 4585-4589). As an example of using the SpRNAi recombinant gene as a source, a SpRNAi-pLNCX2 recombinant gene vector containing homologues to HIV-1 genome from +2113 to +2453 bases was generated following a procedure similar to Example 2. The RNA products (10˜50 μg) of the anti-HIV SpRNAi-pLNCX2 recombinant gene were transcribed from about 106 transfected cells, isolated by RNeasy columns (Qiagen) and then continuously hybrid to its synthetic complementary DNA (cDNA) by heating and then cooling the mixture from 65° C. to 15° C. over a period of 50 min. Transfection was completed following the same procedure shown in Example 5.
Tg(UAS:gfp) strain zebrafish were raised in a fish container with 10 ml of 0.2× serum-free RPMI 1640 medium during transfection. A transfection pre-mix was prepared by gently dissolving 6 μl of a Fugene liposomal transfection reagent (Roche Biochemicals, Indianapolis, Ind.) in 1× serum-free RPMI 1640 medium. SpRNAi-rGFP vectors (20 μg) as described in Example 3 were then mixed with the pre-mix for 30 min and directly applied to the Tg(UAS:gfp) fish. Total three dosages were given in a 12 hr interval (total 60 μg). Samples were collected 60 hr after the first transfection and analyzed by a microscopic quantitation system (Nikon 80i fluorescent imaging;
Zebrafish possesses three FMRP-related genes fmr1, fxr1 and fxr2, which are orthologous to the human FMR1, FXR1 and FXR2 genes, respectively. The expression patterns of these FMRP-familial genes in zebrafish tissues are broadly consistent with those in mouse and human, suggesting that such a loss-of-fmr1-function zebrafish is an excellent model organism for studying the etiology of fragile X mental retardation. We constructed the anti-fmr1 miRNA transgene based on a proof-of-principle design of the SpRNAi-rGFP vector as previously described in the generation of gene-knockout zebrafish (Examples 3 and 9). Because the intronic insert in SpRNAi was flanked with a PvuI and a MluI restriction site at its 5′- and 3′-end respectively, we can remove and replace the eGFP insert with various anti-fmr1 insert sequences possessing relatively cohesive ends to the PvuI and MluI sites. The intronic pre-miRNA insert in this SpRNAi-rGFP vector construct is directed against the nt 25-45 region of the zebrafish fmr1 5′-UTR methylation site (accession number NM152963). This target region contains several 5′-UTR (CGG) repeats, reminiscent of the native anti-FMR1 miRNA target site in human fragile X syndrome.
The anti-fmr1 SpRNAi-rGFP vector was further transfected into 12-hour postfertilization (hpf)-stage zebrafish embryos using the Fugene reagent following the same protocol as described in Example 9 (Lin et al. (2005) supra). The miRNA was expressed under the control of a GABA(A) receptor βZ2 gene promoter in zebrafish brain. After 72-hr post-transfection, zebrafish larvae with the same treatment were homogenized and lyzed using the CelLytic-M lysis/extraction reagent (Sigma Chemicals). Cell lysates were then used in Western blot analysis (
Because the intronic insert in SpRNAi was flanked with a PvuI and a MluI restriction site at its 5′- and 3′-end, respectively, we can change the intronic insert with various anti-gene sequences possessing cohesive ends to the PvuI and MluI sites. We thus transfected chicken embryos with an isolated SpRNAi construct containing a hairpin anti-β-catenin pre-miRNA insert, which was directed against the protein-coding region of the chicken β-catenin gene sequence (NM205081). Using embryonic day 3 chicken embryos, a dose of 25 nM of the isolated SpRNAi construct was injected into the body region close to where the liver primordia would form (
Patched albino (white) skins of melanin-knockdown mice (Rosa-26 black strain) were created by a succession of intra-cutaneous (i.c.) transduction of an isolated SpRNAi-transgene construct directed against the tyrosinase (Tyr) gene for 4 days (total 200 μg). This SpRNAi-transgene construct was designed as described in Examples 3 and 8, except using a hairpin anti-Tyr pre-miRNA insert instead. For efficient delivery into target tissues, the construct was mixed with the Fugene reagent (Roche) following the same protocol as described in Example 9. The gene silencing results were further confirmed by Northern blot analysis as shown in
The following experimentation demonstrates suppression of exogenous retrovirus replication in patient-extracted CD4+ T lymphocytes using the present invention. Specific anti-HIV SpRNAi-rGFP vectors were designed to directly target against the gag-pol region from approximately nts +2113 to +2450 of the HIV-1 genome. This region is relatively conserved and can serve as a good target for anti-HIV treatment. The viral genes located in this target region include 3′-proximal Pr55gag polyprotein (i.e., matrix p17+capsid p24+nucleocapsid p7) and 5′-proximal p66/p51pol polyprotein (i.e., protease p10+reverse transcriptase); all these components have critical roles in viral replication and infectivity.
In order to test the feasibility of using intronic RNA fragments directed against multiple HIV gene targets, the SpRNAi-pLNCX2 proviral vector shown in Example 7 was re-designed to target an early-stage gene locus containing gag/pol/pro viral genes and p24 HIV gene marker. Expectedly, the anti-gag/pol/pro SpRNAi-pLNCX2 transfection will interfere the integration of viral provirus into host chromosome and also to prevent the activation of several viral genes, while the anti-p24 effect will provide a visual indicator for detecting viral activity determined by an ELISA or immunocytochemical (IHC) staining assay. The results showed that such strategy was effective in knocking out exogenous viral gene expression ex vivo in a CD4+ T lymphocyte extract model. Peripheral blood mononuclear cells (PBMC) extracted from patients were purified by CD4+-affinity immunomagnetic beads and grown in RPMI 1640 medium with 200 U/ml IL-2 adjuvant treatment for more than two weeks. An intronic SpRNAi insert containing partial HIV genomic sequence from +2113 to +2453 bases was generated from the SpRNAi-recombinant gene as described in Example 8. After 96 hr incubation, the expression activity of HIV-1 genome was measured by Northern blot analysis (
We transfected human HeLa cells with SpRNAi-rGFP plasmid vectors containing various pre-miRNA* inserts directed against integrin β1 intron 1 nt 43˜68, using the Fugene reagent (Roche), as described in Example 9. HeLa cells, a cervical cancer cell line acquired from ATCC, were grown in DMEM medium supplemented with 10% fetal calf serum at 37° C. with 5% CO2. Thirty-six hours after transfection, total RNAs were extracted using RNeasy spin columns (Qiagen), fractionated on 1% formaldehyde-agarose gels and transferred onto nylon membranes (Schleicher & Schuell). Northern blot analysis was performed as aforementioned in Example 4, except using probes specific for integrin β1 (ITGb1).
The following references are hereby incorporated by reference as if fully set forth herein:
(12) Miyagishi et. al. (2002) U6 promoter-driven siRNAs with four uridine 3′ overhangs efficiently suppress targeted gene expression in mammalian cells. Nat Biotechnol 20: 497-500.
It is understood that the examples and embodiments described herein are for illustrative purposes only and that various modifications or changes in light thereof will be suggested to persons skilled in the art, and are to be included within the spirit and purview of the invention as set forth in the appended claims. All publications and patents cited herein are incorporated herein by reference in their entirety for all purposes.
The present application claims priority to U.S. Provisional Application Ser. No. 60/677,216 filed on May 2, 2005, entitled “Novel Transgenic Animal Models Using RNA Interference” and the present application is a continuation-in-part application of the U.S. patent application Ser. No. 10/439,262 filed on May 15, 2003, entitled “RNA-Splicing and Processing-Directed Gene Silencing and the Relative Applications Thereof”, which are hereby incorporated by reference as if fully set forth herein.
This invention was made with support in part by a grant from NIH (CA 85722). Therefore, the U.S. government has certain rights.
| Number | Date | Country | |
|---|---|---|---|
| 60677216 | May 2005 | US |
| Number | Date | Country | |
|---|---|---|---|
| Parent | 10439262 | May 2003 | US |
| Child | 11278143 | Mar 2006 | US |
